Rentenkasse- Antrag auf Erwerbsminderungsrente

Fibromyalgie – Erwerbsminderungsrente

Wegen einer Erkrankung wie die Fibromyalgie eine Erwerbsminderungsrente zu beantragen erfordert viel Geduld

Wenn man aus gesundheitlichen Gründen nicht mehr arbeitsfähig ist, gibt es die Möglichkeit eine teilweise oder volle Erwerbsminderungsrente zu beantragen, auch wenn man das Alter für die Altersrente noch nicht erreicht hat. Wegen einer Fibromyalgie eine Erwerbsminderungsrente zu beantragen ist und bewilligt zu bekommen ist unverhältnismäßig schwer. Ich habe nur mit sehr schwerem Herzen und in einem langen schmerzhaften Prozess realisiert, dass ich aufgrund meiner Fibromyalgie nicht mehr in der Lage bin zu arbeiten. Mein Beruf war mein Leben, bis zum Schluss war ich mit viel Engagement und Leidenschaft dabei. Mir war schon lange bewusst, dass der Beruf der Erzieherin enorm anstrengend ist und hochgradiger Stress, auch für meine jungen und gesunden Kolleg*innen. Ich hatte mir einen Status erarbeitet, mit dem ich durch Zusatzausbildungen das Zeug dazu hatte Eltern zu beraten oder in die Erwachsenenbildung zu wechseln und Erzieher*innen auszubilden. Jede*r der mich kennt, weiß wie gerne ich gearbeitet habe.

Antrag auf Erwerbsminderungsrente – eine schwere Entscheidung.

Die Entscheidung wegen der Fibromyalgie eine Erwerbsminderungsrente zu beantragen wurde mir auch noch zusätzlich erschwert, weil sämtliche Ärzt*innen und meine Therapeutin mir wenig Hoffnung auf Erfolg machten. Tatsächlich ist es viel einfacher ein Rente bewilligt zu bekommen, wenn man zum Beispiel an einer Depression erkrankt ist. Im Frühjahr 2015  habe schweren Herzens und nach langem und hin und her einen Antrag auf Erwerbsminderungsrente gestellt. Mein Antrag wurde abgelehnt, aber damit hatte ich ja gerechnet.

Ich habe Widerspruch eingelegt und  musste nach langem Warten ein halbes Jahr später zu einer Begutachtung. Ein Neurologe und Psychiater lud mich zur Begutachtung ein .Ich versuchte mich auf den Termin vorzubereiten, habe aber schnell festgestellt, das ich mit diesem Gutachter kein Glück haben werde. Der Termin nimmt mich leider extrem mit. Ich kann es nicht leiden, durchleuchtet zu werden, Fragen gestellt zu bekommen, die ich niemals ohne weiteres einem fremden Menschen beantworten würde. Fragen zu meiner Lebenssituation, zu meiner Familie, meinen Eltern, meinen Kindern und meinem Lebensgefährten. Fragen die unter Umständen sehr intim sind. Ich bin dem Rat meiner Anwältin gefolgt und habe alle Fragen ehrlich und mit guten Gewissen beantwortet. Der Gutachter hatte eine höchst unangenehme Art, er stellte die Fragen, indem er dauernd sprunghaft das Thema wechselte und mich von oben herab behandelte. Und es dauerte keine fünf Minuten, da hat er mir klar gemacht, dass Fibromyalgie nicht gäbe.

Das Ergebnis dieses Gutachtens war: Wenn ich mich endlich einer psycho-pharmakologischen Behandlung unterziehe bin ich bald wieder arbeitsfähig. Der Widerspruch wurde abgelehnt!

Das ist natürlich völlig absurd, weil ich nicht an einer Depression erkrankt bin und auch keine Persönlichkeitsstörung habe, sondern ein Fibromyalgie – Syndrom , dessen Ursache im Grunde noch nicht weitreichend erforscht ist. Man spricht zwar von einer psychosomatischen Erkrankung, aber wie hoch der seelischer Anteil ist und inwieweit organische Ursachen vorliegen, weiß man bis heute noch nicht.

Der Widerspruch wurde auch abgewiesen

Jetzt musste ich mich entscheiden, gebe ich dem nach und versuche eine berufliche Alternative zu finden oder will ich gegen die Rentenkasse klagen. Die Entscheidung war klar, weil ich mit Sicherheit nicht mehr arbeiten kann. Die Klage wurde durch meine Anwältin beim Sozialgericht eingereicht und dann hieß es wieder warten.Und jetzt wollte ich erst recht gewinnen. Ich wollte „beweisen“, dass es die Fibromyalgie gibt und man auch wegen Fibromyalgie eine Erwerbsminderungsrente beantragen kann.

Nachdem ich mehrere Monate vergeblich auf eine neue Begutachtung wartete, musste die dafür beauftragte Ärztin erst noch vom Sozialgericht aufgefordert werden. Dann endlich bekam ich wieder eine Einladung zur Begutachtung. Diesmal beauftragt vom Sozialgericht. Und auch dieses Mal wurde die Begutachtung durch eine Fachärztin für Neurologie und Psychiatrie durchgeführt.

Jetzt saß ich bei einer Frau, die ich zunächst als angenehmer und empathischer empfunden hatte, als der Arzt bei der ersten Begutachtung. Trotzdem war auch dieser Termin für mich der Horror. Sie hat mich in ähnlicher Weise über mehrere Stunden befragt, danach hat sie mich untersucht um einen allgemeinen Gesundheitszustand festzustellen und anschließend musste ich noch diverse Fragebögen ausfüllen.

Danach war ich fix und fertig und hätte am liebsten nur noch geheult. Schon auf der Heimfahrt war mir klar, das auch dieses Gutachten nicht zu meinem Gunsten aus fallen wird. Das Gespräch und die Befragung von dieser Ärztin ging im Grunde genommen in die gleiche Richtung, wie beim ersten Mal. Meine Beeinträchtigung durch die Fibromyalgie wurde extreme in Frage gestellt. Im Grunde war diese Sub – Botschaft: Fibromyalgie ist eine eingebildete Krankheit die es nicht gibt! Vielmehr sind meine Verhaltensweise und Charakterschwächen Grund für meine Schmerzen und arbeitsfähig bin ich dann, wenn ich eine Einsicht habe und mich bemühe meine Schwächen zu erkennen.

Sie hat alle von mir beschriebenen Symptome nicht ernst genommen und stattdessen meine äußerliche Erscheinung als Indiz dafür genommen, dass es mir gut geht und ich arbeitsfähig bin. So schreibt sie z.b. unter der Rubrik „allgemeiner Gesundheitszustand“ .… Die Klägerin hat rot lackierte Fußnägel, trägt Schmuck und hat ein gebräuntes Dekolleté!

Sieht so ein professionelles Gutachten aus?

Ich finde es äußerst fragwürdig, vom äußerlichen Erscheinungsbild auf eine Erkrankung zu schließen bzw. aufgrund meines gepflegten Aussehens eine Beeinträchtigung auszuschließen. Darf ich nicht gepflegt aussehen, weil ich chronische Schmerzen habe? Muss ich mich für meine Körperpflege entschuldigen? Meiner Meinung nach sind solche Äußerungen im Kontext einer gutachterlichen Aufgabe absolut unangemessen und nicht gestattet. Ich empfinde sie als höchst diskriminierend.

Aber das ist längst noch nicht alles. Mehrere Hinweise in dem Gutachten, die ich als diskriminierend empfunden habe und mit dem ich mich nicht einverstanden erklären kann.

Sie kommt zum Beispiel zu dem Ergebnis, dass ich zwar Schmerzen habe, aber keine Beeinträchtigungen durch die Schmerzen. Denn wenn ich in der Lage bin, zweimal in der Woche 15 Minuten Yoga und 15 Minuten Nordic Walking machen kann, bin ich auch arbeitsfähig.

Sie schreibt in dem achtzehnseitigen Gutachten: „Hier ist zu konstatieren, dass die Angabe einer chronischen Erschöpfung bei Durchsicht des Berichtes und Angaben, dass die Klägerin zweimal wöchentlich Nordic Walking machen 15 Minuten täglich Yoga übe und häufig Fahrrad fahre, kritisch zu hinterfragen ist.“

und an anderer Stelle heißt es:

„….Die Klägerin kann von Fortführung intensiv Physio- als auch Sport therapeutischer Maßnahmen, vom copingmechanismen im Umgang mit chronischen Schmerzen als auch stationäre multimodale schmerztherapeutischen Behandlungsansätze profitieren….“

Tatsache ist, dass diese von mir geschilderten Aktivitäten Teil eines von vielen Ärzten empfohlenen Therapieprogramms sind. Die Fachliteratur spricht von einem multi-modalen Behandlungskonzept, gemeint ist eine Kombination aus Bewegungstherapie, Medikamenten, individueller physikalischer Therapie, Entspannungsverfahren und falls notwendig Psychotherapie. Und in diesem Sinne sind auch meine Aktivitäten zu betrachten. Ich versuche tagtäglich durch die mir empfohlen Therapien trotz meiner Schmerzen eine gewisse Lebensqualität zu erhalten. In der Realität sieht es aber so aus, dass ich an manchen Tagen keinen einzigen Teil dieser „Selbsttherapie“ durchführen kann.

An mindestens drei von sieben Tagen kann ich weder mein Yoga machen, noch irgendeine andere sportliche Tätigkeit durchführen, weil mir die Kraft dazu fehlt.

Da meine Schmerzen auch oft in Schüben auftreten, kann ich phasenweise so gut wie gar nichts machen. Im Moment kann ich schon seit mehreren Wochen nicht mal mehr Fahrrad fahren, was bisher für kurze Strecken einigermaßen machbar war. Dadurch bin ich in meiner Mobilität noch mehr eingeschränkt. Unklar ist, ob ich jemals wieder Fahrrad fahren kann, um nur ein Beispiel zu nennen.

Aber ich gebe den Kampf mit der Rentenkasse nicht auf. Ich will die Erwerbsminderungsrente aufgrund meiner Fibromyalgie bewilligt bekommen! Noch habe ich Mittel, die mich hoffen lassen, dass ich am Ende meine Rente bewilligt bekomme. Mein Glück ist, dass ich eine Rechtsschutzversicherung habe und ich ein weiteres Gutachten erstellen lassen konnte. Falls ich den Prozess verliere, wird mich das 1500 € kosten, was hoffentlich nicht der Fall sein wird.

Leider musste ich auch dieses Mal mehrere Monate auf die Einladung zu einer Begutachtung warten. Diesmal hat das Gutachten Facharzt für Schmerztherapie erstellt. In diesem Gespräch hatte ich zum ersten Mal mit einem Menschen zu tun, der nicht herablassend unvoreingenommen war. Im Gegenteil, dieser Arzt hat mir zunächst die Richtlinien, nach denen ein Gutachten verfasst werden muss erklärt, nachdem er mir ein Glas Wasser anbot und mir sagte, dass er gerne ein Gespräch auf Augenhöhe mit mir führen möchte. Die Fragen waren eigentlich ähnlich derer, die ich in den anderen beiden Gesprächen schon gestellt bekommen hatte, aber der Habitus war ein ganz anderer. Außerdem tippte der Arzt meine Antworten direkt in den Computer, las mir vor was er geschrieben hatte fragte mich ob das okay sein. Ich konnte sehr schnell feststellen,  dass er Erfahrungen mit der Krankheit  Fibromyalgie hat und er die Erkrankung gut kennt. Aufgrund meiner Krankheitsgeschichte und den von mir geschilderten Symptome war er der Meinung, dass ich nicht mehr arbeitsfähig bin. Das Gutachten ist nicht nur zu meinen Gunsten ausfallen, es belegt auch eindeutig, das meine von mir beschriebenen Schmerzen die der messbaren Schmerzen entspricht. Nicht nur das, es berücksichtigt auch meine lange Krankheitsgeschichte.

Immer noch keine Entscheidung vom Sozialgericht

Seit Antragstellung sind jetzt fast fünf Jahre vergangen und manchmal geht mir diese Warterei sehr an die Nieren. Nicht zu wissen was mich in der Zukunft erwartet ist fürchterlich und raubt mir nicht selten meine nächtlichen Schlaf. Ich weiß dass die Sozialgerichte in Berlin hoffnungsvoll überlastet sind, so dass ich davon ausgehen kann, das ganze Prozedere noch mindestens ein halbes Jahr dauern wird. Mit dieser Ungewissheit zu leben macht mich richtig fertig. Vor allem weil ich nicht weiß, was ich machen soll wenn ich wieder abgelehnt werde. Aber daran will ich jetzt erstmal nicht denken.

Ich bin froh, dass ich mich zu diesen Schritten entschieden habe und will auf keinen Fall aufgeben. Es macht mich auch ein bisschen stolz, dass ich der Rentenkasse die Stirn bieten kann. An manchen Tagen fühle ich mich deshalb besonders stark, trotz meine Erkrankung!

12.333 Kommentare

  1. Ich habe Tränen in den Augen, als ich die Geschichte gelesen habe. Sie ist meiner so ähnlich. Auch wurde bei mir im Gutachten ebenfalls von rot lackierten Fußnägeln und gepflegter Erscheinung berichtet. Ausserdem wurde angemerkt, dass ich wegen der Fibromyalgie noch keine Abmahnung von meinem Arbeitgeber bekommen habe. Es ist eine große Firma mit sozialer Einstellung, da macht man das halt nicht. Eine absolute Unverschämtheit! Am liebsten hätte ich diesen Scharlatan nochmal besucht. Ich bin gerade dabei, auf einen GdB >=50% zu kommen und hatte wieder einmal einen Gutachtertermin wegen einer Klage vorm Sozialgericht. Ausgang ist noch offen. Nächste Woche habe ich einen Gutachtertermin wegen der beantragten EMR . Vor ein paar Jahren habe ich eine Rechtschutzversicherung abgeschlossen und mache das seit letztem Jahr nur noch mit Anwältin. Ohne klappt gar nichts. Dafür hat man sich ein Leben lang abgerackert und Beiträge gezahlt. Seit über 10 Jahren versuche ich einen GdB über 30 % zu bekommen. Die wollen einen nur mürbe machen und ich wünsche denen 1 Tag Fibro, damit die ihre blöde Klappe halten.
    Wann ändert sich das endlich?😖😭

    • Liebe Silke,
      Vielen Dank für deinen ausführlichen Kommentar! Zunächst muss ich mich bei dir entschuldigen, weil ich jetzt erst reagiere….das tut mir wirklich sehr leid! Ich hatte im Mai eine schwere Rücken – OP, von der ich mich so langsam erhole. Dazu kommt, dass mir in Bezug auf meinen Blog ein wenig die Puste ausgegangen ist, weshalb ich schon lange keinen Beitrag mehr geschrieben habe. Zum einen hat das mit Corona zu tun gehabt und zum anderen mit meinen verflixten Rückenschmerzen, die mich schier lahmgelegt haben. Meine Situation hat sich aktuell zusätzlich dramatisch verschlechtert. Auch ich musste erneut zum Gutachter, dieses mal vom Sozialgericht angeordnet zu einem Orthopäden. Der Termin bei ihm und das Gutachten, welches ich vor einigenTagen per Post bekommen habe, ist ein einziges Desaster. Darüber werde ich in jedem Fall einen Beitrag schreiben, denn ich finde,dass es unbedingt an die Öffentlichkeit gelangen muss, was Menschen mit Fibromyalgie, die nicht mehr arbeitsfähig sind, widerfährt. Auch deine Geschichte macht mich sprachlos und wütend. Ich habe immerhin eine Schwerbehinderung von 50% anerkannt bekommen, allerdings habe ich 10 Jahre darum gekämpft. Inzwischen habe ich auch den Pflegegrad 1, nur sind viele meiner Einschränkungen nicht berücksichtigt worden. Laut der Berechnung der Leiterin (mit entsprechend jahrelanger Erfahrung) eines Pflegestützpunktes stünde mir ganz sicher sogar der Pflegegrad 2 zu. Mit der Veröffentlichung meiner Geschichte kämpfen ich auch für mehr Anmerkungen für alle Menschen mit Fibromyalgie!
      Ich gebe dir recht: wann hört das endlich auf!!!!

    • Ich kenne das aus eigener Erfahrung. Man wird für faul gehalten. Ein Arzt hat zu mir gesagt ,, es sind Frauen ydie weder an Gott glauben noch bereit sind den Anforderungen zu genügen. Der VDK hat mir mit Rechtsanwälten geholfen meine Rente zu erhalten
      Im Moment Kämpfe ich um Anerkennung zur Pflegestufe. MeinFMS hat sich für einen neuen Schub entschieden.

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